Age-Dependent Hematologic Toxicity Profiles and Prognostic Serologic Markers in Postoperative Radiochemotherapy Treatment for Uterine Cervical Cancer

Introduction: In the adjuvant setting for cervical cancer, classical risk factors for postoperative radiochemotherapy have been established. However, data on laboratory changes during therapy and the prognostic value of serological markers are limited and further knowledge is needed to optimize the toxic trimodal regimen. Methods: We retrospectively identified 69 women who underwent weekly postoperative radiochemotherapy with 40 mg/m2 of cisplatin for cervical cancer between 2010 and 2021 at a single center. Laboratory parameters were recorded before, at each cycle and after radiochemotherapy. Kaplan-Meier and log-rank analyses were used to calculate and compare survival, groups were compared using the Mann–Whitney U, χ2, and variance tests. Results: With a median follow-up of 17.7 months, the 1- and 5-year local control rates were 94.0% and 73.7%, respectively, with significantly better rates for more chemotherapy cycles and negative resection margins. Only 68.1% of patients completed all cycles. The most common reasons for early discontinuation were persistent asymptomatic leukopenia in women aged ≤ 50 years, and limiting infections in women aged > 50 years. Leukopenia was more likely to occur after the third cycle. Significantly worse survival was observed for post-radiochemotherapy elevated C-reactive-protein and lactate dehydrogenase levels, low pre-radiochemotherapy nutritional index, and raised C-reactive-protein-levels; the latter were also predictable for local control. The Glasgow prognostic score did not reliably predict survival. Conclusion: Incomplete application of simultaneous chemotherapy leads to inferior local control, and age-dependent limiting factors should be identified at an early stage. In addition to classical risk factors, serological markers (C-reactive-protein, lactate dehydrogenase, nutritional index) show prognostic significance.


Introduction
Cervical cancer accounts for both, the fourth most frequently diagnosed cancer and the fourth leading cause of cancer death in women with 604 000 new cases and 342 000 deaths in 2020. 1 The implementation of vaccination against human papilloma virus and screening methods effectively led to the reduction of incidence and mortality, as well as the detection of earlier stages. [2][3][4] In managing early-stage cervical cancer, defined as Federation of Gynecology and Obstetrics (FIGO) stages 1A-1B, fertility-sparing surgery or radical hysterectomy represents the cornerstone of curative therapy, whereas for higher stages, definitive radiochemotherapy (RCHT) is the treatment of choice. [5][6][7] Overall survival (OS) rates decrease with higher stages, from 4-year OS rates of approximately 98.2% and 97.0% for FIGO stages 1A-1B1, to 83.1% for stage IB3, and poor 5-year OS outcomes of 46.0% for stage IIIA and 5.1% for stage IVA. [8][9][10] In addition to FIGO stage, positive nodal status, deep stromal and lymphovascular space invasion (LVSI), histologic subtype of adenocarcinoma, and higher grade are considered high-risk factors, and appear more often in larger tumors. [11][12][13][14][15][16] For FIGO 1A, there is a risk for the presence of pelvic lymph node metastases of only 3.5% to 7.4%, and the presence of LVSI significantly reduces tumor control. [8][9][10][11][12][13][14][15][16][17] The need for adjuvant therapy after surgery for early-stage cervical cancer with unfavorable pathological criteria has been widely investigated with proof of superior local control (LC) and progressionfree survival, when postoperative RCHT was applied compared to surgery alone. 15,18,19 This has been proven for high-risk "Peters" criteria with positive lymph nodes, involved surgical margins or parametrial infiltration and intermediate-risk "Sedlis" criteria with large tumors > 4 cm, deep stromal infiltration or lymphangiosis. 18,19 The addition of postoperative concurrent chemotherapy showed significantly improved progression-free and OS in the adjuvant high-risk setting in the Gynecologic Oncology Group (GOG 109) trial, and concurrent cisplatin-based schemes are currently the standard of care as it has the least toxicity among various chemotherapy regimens. [19][20][21] Nevertheless, there is evidence that only patients with multiple lymph nodes or histologic subtype of squamous cell carcinoma may benefit from adjuvant chemotherapy. 12,22 The assessment of risk factors remains controversial and heterogeneous, and the STARS trial 23 further questions the sequence of the optimal chemotherapy administration, preferring a sequential application more than concurrent regimens. Furthermore, late toxicity encompassing proctitis, diarrhea, bowel inflammation, fistula or stenosis, ulceration, and toxicity within the urinary bladder, such as cystitis, is significantly higher in patients with trimodality treatment (surgery, radiotherapy [RT], chemotherapy) with severe events in 7% to 15.3% of patients, compared to surgery plus RT alone in 2% to 5.5% of patients; 11,12 thus, critical patient selection for prevention of overtreatment or undertreatment is still needed.
In terms of optimizing treatment and prognosis prediction, additional prognostic biomarkers with serologic data and the systemic inflammatory immune response focusing on preoperative peripheral blood cell ratios have emerged, showing prognostic values of neutrophil, monocyte, and lymphocyte ratios for predicting OS in cervical cancer. 24,25 Furthermore, serological laboratory markers with elevated lactate dehydrogenase (LDH) levels have been shown to be associated with inferior survival in cervical cancer and endometrial cancer. 26,27 In this study, we aimed to evaluate the impact and effectiveness of concurrent cisplatin-based chemotherapy on oncologic outcomes, and investigate the toxicity profile of high-risk subgroups to improve multimodal treatment. Furthermore, we aimed to explore the impact of additional prognostic serologic biomarkers and provide new evidence of serological markers at different time points during RCHT treatment.

Materials and Methods
In this single-center retrospective study, we analyzed women, who were treated with postoperative radiotherapy and simultaneous weekly cisplatin for cervical cancer between October 2010 and August 2021. The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the local ethical review board (approval number: S-453/ 2021). The requirement for informed consent from each individual was waived by the appropriate institutional review board. All patient details and personally identifiable information were de-identified.
Only patients in an adjuvant curative setting with upfront oncologic surgery including hysterectomy and at least pelvic lymphadenectomy, application of postoperative pelvic RT plus simultaneous chemotherapy with weekly cisplatin, and complete laboratory data were included. Treatment concepts were determined in multidisciplinary tumor conferences according to each patient's individual risks and cases with neoadjuvant chemotherapy or palliative treatment regimens were excluded. Patient, treatment and oncologic data were individually assessed. Staging included computed tomography (CT) of the thorax and magnetic resonance imaging of the pelvis, with further classification according to the FIGO 2018 staging system 5 and eighth edition of the TNM American Joint Committee on Cancer staging system.

Radiotherapy
External beam radiotherapy (EBRT) was delivered using 6 MV photons and intensity-modulated radiotherapy (IMRT) alone or in combination with brachytherapy (BT). Contouring was performed on 3 mm slice thickness CT planning imaging and delineation according to guidelines and adapted to each patients' individual risk. Dose constraints for adjacent organs at risk were in accordance with the Quantec recommendations. 28,29 The clinical tumor volume (CTV) included the pelvic region with the vaginal cuff, the upper vagina, parametrial and paravaginal tissues and nodal irradiation consisting of external and internal iliac, common iliac, obturator, and presacral regions up to the bifurcation of the aorta. The para-aortic region was only included in case of para-aortic lymph metastases. A planning target volume (PTV) with a margin of 0.5 to 2 cm to the CTV was added. The prescribed dose to the PTV for EBRT was 45 to 54 Gy delivered once daily in 25 to 30 fractions, for a treatment time of 5 to 6 weeks. For macroscopic lymph node metastases, a simultaneously integrated boost (SIB) of 54 to 58.8 Gy was applied. Women with high-risk factors, such as lymphangiosis or microscopic residual vaginal tumor, received a vaginal cuff high-dose-rate (HDR) BT, using iridium-192 with an intracavitary single applicator according to Brachytherapy Consensus Guidelines 30 with single doses of 5 Gy in 1 to 3 fractions. For further comparison, EBRT and HDR brachytherapy boost doses were converted and summed in an equivalent dose in 2 Gy fractions (EQD2) using the linear quadratic model. An α/β ratio of 10 was assumed for the tumor. EQD2 (Gy) = fractional dose × number of fractions × (fractional dose + a/β)/(2 Gy + a/β)].

Chemotherapy and Peripheral Blood Cell Counts
Cisplatin was administered in a weight-dependent manner (40 mg/m 2 ) with 250 ml of intravenous isotonic saline once weekly. The number of intended cycles depended on the duration of EBRT, leading to a total target dose of 200 to 240 mg/m 2 in 5 to 6 cycles. Supportive antiemetic pre-medication using corticosteroid prophylaxis, granisetron, and aprepitant was given intravenously 2 hours prior to chemotherapy and the following days depending on the individual status and extent of emesis. Before, during, and after chemotherapy, at least 2000 ml of isotonic saline with magnesium, potassium, and 15% mannitol was administered over 6 to 8 hours. Hydration infusion therapy was additionally used in between cycles for nephroprotection.
Patients were assessed for reduced cardiac function, hearing deficits, infections, and general clinical performance status before administration and re-evaluated during the course of treatment. Biochemistry laboratory values and weights were documented before and after each cycle. Dose reduction or hematopoietic stimulation was not routinely performed. Upcoming cycles were omitted or delayed in the presence of persistently low counts of leukocytes (<3/nl), platelets (<100/ nl), and symptomatic anemia with hemoglobin levels <8.5 g/ dl, in cases of acute kidney failure or inadequate glomerular filtration rate (GFR) using the Cockcroft-Gault formula, fulminant infection, or deterioration of clinical performance status. Routine laboratory data analysis was performed for white cell and platelet counts, hemoglobin levels, and GFR and documented before and after each chemotherapy cycle.

Serologic Markers and Nutritional Assessment
Baseline and weekly values were assessed before and after RCHT and at each time point of chemotherapy for body weight and body mass index (BMI [kg/m 2 ] = weight/height × height), C-reactive protein (CRP), serum albumin, and LDH levels.
We determined the scores of the nutritional index (NI = albumin/CRP) 31 and the Glasgow prognostic score (GPS) 32 with grouping of CRP and albumin concentrations into 3 categories with zero points for the best prognosis and values in the normal ranges up to 2 points with the worst prognosis, with elevated CRP combined with hypoalbuminemia.

Oncologic Outcomes
For each patient, the evaluation of treatment response included follow-up visits with clinical data, referring physician notes, and radiology. Clinical outcomes included the assessment of OS, LC, and distant control (DC). OS was defined as the period from the first day of radiotherapy until the last contact or date of death. LC was considered until any tumor progression at the original site or local pelvic lymph nodes, while DC was defined as metastatic lesions developing outside the pelvis. Common Terminology Criteria for Adverse Events (CTCAE; version 5.0) were used for the grading of acute (<90 days) and late (≥ 90 days) toxicity.

Statistical Analysis
Kaplan-Meier analysis and the log-rank test or Cox regression were utilized to calculate survival curves and compare subgroups, with statistical significance set at P < .05. Univariate and multivariate Cox proportional hazard ratios (HRs) and 95% confidence intervals (CIs) were used to assess the influence of cofactors. Patient and treatment characteristics as well as laboratory data were compared using the Mann-Whitney U-test or Pearson chi-square test for continuous or categorical data and analysis of variance with repeated measures and the t-test, respectively. Statistical analyses were performed using SPSS (version 28.0; Chicago, Illinois).

Results
Out of 99 women, who were treated with curative, postoperative RCHT following surgical resection for cervical cancer at our institution between October 2010 and August 2021, 69 patients with a median age of 48 (range: 12-78) years met our inclusion criteria. Pelvic IMRT was applied with a median dose of 45.0 (range: 32.4-54.0) Gy and a median number of 25 (range: 10-30) fractions, with a median SIB dose of 55.5 (range: 54.0-58.8) Gy. One patient had to stop RT after 10 fractions due to infection and refused to continue therapy after recovery. Detailed patient and treatment characteristics are listed in Table 1.
Patient and treatment characteristics for patients aged ≤ 50 and > 50 years were comparable in terms of demographic parameters as listed in Table 1, except for significant differences regarding the baseline GFR (P < .001), which were significantly lower in older patients.

Serological Prognostic Factors
Pre-RCHT lowered values of the nutritional index (HR 0.996 [CI: 0.993-0.999], P = .016) and raised pre-RCHT CRP levels (HR 1.042 [CI: 1.013-1.072], P = .004) were significantly correlated with a worse OS. The GPS tended but did not reliably predict survival (HR: 2.756 [CI: 0.949-8.000], P = .062). Factors strongly linked to inferior OS at the end of RT were elevated post-RCHT CRP (HR 1.015 [CI: 1.001-1.030], P = .031) and LDH levels (HR 1.010 [CI: 1.000-1.020], P = .050). Pre-RCHT raised CRP levels were also predictable for LC (HR 1.040 [CI: 1.001-1.080], P = .045). Neither did the pre-post-RCHT ratios of CRP, LDH, and albumin predict OS, LC or DC, nor the ratios of the blood counts. Table 2 presents a detailed analysis of the prognostic impact on oncologic outcomes. Figure 2 shows the values of hemoglobin levels, leukocyte and platelet counts, BMI, body weight, and GFR at baseline at the time point of cycle one and over the course of cisplatin RCHT treatment.
Platelet counts ( Figure 1C) significantly decreased after the second cycle (P = .047), while thrombocytopenia (grade 1, platelets below 100/nl) was only present in 3 patients (4.3%) in the sixth cycle (P < .001). None of the patients underwent platelet transfusions. There was no higher grade (≥2 grade as defined by ≤74.9/nl) thrombocytopenia present during chemoradiation.
GFR ( Figure 1D) was significantly reduced at the time point of the sixth cycle (P = .009). Of note, renal failure limited the application of chemotherapy in 2 patients, while 4 patients suffered from acute renal failure after the end of treatment after completion of all intended cycles (5 cycles: n = 3, 6 cycles: n = 1), leading to chronic renal failure in 2 cases. No significant changes in the BMI ( Figure 1E) or absolute body weight ( Figure 1F) were observed over the course of RCHT treatment. The comparison of values at baseline and after the last chemotherapy cycle for the whole cohort showed a median pre-/ post-treatment reduction of −9.5% (range: −38.8% to + 37.9%) for hemoglobin levels, −48.9% (range −81.2% to + 94.8%) for leukocyte counts, −41.1% (range: −66.3% to + 61.0%) for platelet counts, −1.4% (range: −64.9% to + 16.7%) for the GFR and −0.9% (range: −11.6% to + 8%) for the BMI and body weight. The reduction in GFR was significantly higher (P = .036) in older patients over 50 years than in the younger cohort. The median values and ranges of the absolute and percentage changes in laboratory data for each age-dependent subgroup are listed in detail in Table 3.
Administration of 5 cisplatin cycles with a cumulative target dose of 200 mg/m 2 was intended for 38 patients (55.1%) and 6 cycles with a cumulative target dose of 240 mg/m 2 for the remaining 31 women (44.9%). Twenty-two patients (31.9%) did not complete this chemotherapy regimen as planned, which was due to one or a combination of the following: persistent leukopenia (n = 12), limiting infections (n = 9), and irreversible renal failure (n = 2). The reasons for early cessation of chemotherapy were significantly age-dependent with asymptomatic persistent leukopenia more often in the younger subgroup (≤50 years, n = 11, P = .011) and limiting infections in women over 50 years of age (n = 8, P = .011).

Discussion
Avoiding toxicity in the trimodality concept is an important issue in curative adjuvant RCHT treatment for cervical cancer. The application of simultaneous chemotherapy can lead to severe side effects, while omission can limit oncologic outcome. This study aimed to identify high-risk subgroups and evaluate toxicity profiles and oncologic outcome. Our results underline the importance of age-dependent monitoring of chemotherapy-limiting toxicity profiles of women in the adjuvant treatment of cervical cancer and provide new quantitative evidence on weekly reductions in peripheral blood cell counts and an analysis of prognostic serologic markers and indices as predictive tools that have so far not been assessed for applicability in this entity.
As the impact of heterogonous risk factors on prognosis remains controversial, the inclusion of personalized biomarkers is of great interest to provide more accurate information on prognosis and tracking of therapy. Currently, there are no such strongly validated tumor markers for widespread clinical use for cervical cancer. The evaluation of a causal link between elevated biomarkers due to consecutive alterations in tumor microenvironment and inferior outcome and thus the inclusion of serologic markers is of great interest for prognosis stratification.
Lower pretreatment LDH levels have recently been shown to highly reflect a patient's superior prognosis in the treatment of small cell lung cancer undergoing platinum chemotherapy, in patients with head and neck tumors and lymph node positive prostate cancer as well as uterine cervical cancer. 26,[33][34][35] In our study a higher LDH level at the end of RCHT treatment was a predictive marker for inferior OS; interestingly, this could not be proven for baseline or pre-RCHT LDH levels. Previous studies have hypothesized that the metabolic cause of elevated LDH levels in patients with poorer outcomes is related to the presence of increased hypoxia due to the enzyme's function in anaerobic conditions. 34,36 In more detail, elevated serum LDH release in cancer patients has been shown to be correlated with LDH-isoenzyme-5 expression in tumor tissue; furthermore, increased LDH-isoenzyme-5 expression is linked to higher chemo-and radiotherapy resistance and has been reported to be an independent negative prognostic marker in endometrial cancer. 27,37,38 In addition, the connections between anemia and tumor hypoxia to tumor progression, especially in the context of radiotherapy and tissue microenvironements are highly important for radio-and chemotherapy resistance. 38 Hemoglobin levels of 12 to 14 g/dl have been considered optimal for tumor therapy, but reliable oxygen measurement tools have so far not been described. 39 Our study did not find any association between hemoglobin levels and tumor control at any time point or at pre-post-RCHT ratios. Regarding locally advanced cervical cancer, preoperative and pre-/post-radiotherapy LDH and CRP levels have been found to be independent markers for OS and progression-free survival in the definitive and neoadjuvant setting and with a higher predictive value in human papillomavirus-positive cervical cancer. [40][41][42][43] However, so far prior studies have not focused on the evidence for a reliable transferability of this to the adjuvant situation as presented in our cohort. The OS in our study was considerably inferior predicted by pre-and post-RCHT CRP levels, post-RCHT LDH levels, and pre-RCHT values of the nutritional index.
Of note, serologic markers cannot be analyzed without focusing on the toxicity of both chemotherapy and radiotherapy and their impact on laboratory changes. The use of 3-dimensional RT techniques using concurrent weekly cisplatin 40 mg/m 2 resulted in high rates of grade ≥3 acute hematologic toxicity and 19% acute lower gastrointestinal toxicity, but comparable 3-year OS of 90% and LC of 88%. 21 The application of advanced and widespread pelvic IMRT techniques as used in our study, however, can lower the rates of hematologic toxicity without diminishing the oncologic outcome. The RTOG 0418 trial of Klopp et al 44 investigated the impact of the RT dose on the hematopoietic stem cell compartment and found an improved bone marrow sparing in a group of women who received postoperative RCHT and radiotherapy for cervical (n = 40) and endometrial cancer (n = 43) to be significantly associated with lower rates of hematotoxicity. Volume-dose constraints to the bone marrow of V40Gy≤37% with a mean dose below 34.2 Gy were suggested to decrease the reduction in peripheral blood cell counts. Interestingly, these hematotoxicities were not linked to the number of chemotherapy cycles applied in the cervical cancer subgroup. Our cohort consisted of a large subgroup of women with higher stage FIGO stage 3 + 4 (44.9%) patients after surgery, and we confirmed known classical pathologic high-risk factors of lymphangiosis, positive tumor margins, or larger tumors. 18,19 The resulting 5-year rates of OS and DC were 52.5% and 50.5%, respectively, and thus comparable to prior studies of approximately 51.6% after chemoradiation in highrisk patients, but were overall poor and further improvement for oncologic outcomes is greatly needed. 8,9,11 In the context of poor DC, the addition of consolidation chemotherapy to adjuvant concurrent RCHT may be the key to further improvement. In the ACTLACC trial, 45 patients who received consolidation paclitaxel plus carboplatin after RCHT had a significant benefit in systemic recurrence-free survival. Zhong et al 46 further confirmed the advantage of multiagent consolidation chemotherapy for high-risk cervical cancer patients for diseasefree survival and OS, but with an association of increased highgrade rates of myelosuppression. Sun et al 47 even had to stop a randomized phase III trial for the evaluation of topotecan plus cisplatin in the postoperative setting due to severe hematologic toxicity. The use of a triweekly cisplatin-alone regimen was proven to have the same oncologic outcome, but was more toxic than weekly cisplatin in a study by Lee et al, 48 while Zhu et al 49 showed a slightly better outcome for disease-free survival at the cost of significantly more high-grade leukopenia.
The 5-year pelvic recurrence-free survival rate was 77.3% in an analysis by van den Akker et al 11 and thus in line with the results of our study with a 5-year LC of 73.7%. The same was found with comparable local recurrence rates of 11.6% in our study compared to 13.9% reported by Rotman et al. 15 As concurrent chemotherapy could be proven as an independent prognostic factor for superior LC, we strongly advocate for the application of full-course cycles, whenever clinically feasible, as meta-analyses have also revealed the effectiveness of postoperative RCHT for improved OS, LC, and DC compared to adjuvant RT alone especially for lymph node-positive patients. 50,51 While there is still an international consensus on adjuvant RCHT in high-risk patients, the results of the STARS trial of Huang et al 23 have reopened the controversial discussion regarding the optimal sequence of adjuvant treatment. In their study, sequential chemoradiation led to higher disease-free-survival and a lower risk of cancer death compared to concurrent RCHT regimes. Furthermore, targeted therapies are increasingly dominating the treatment of cervical cancer and could offer additional attractive future treatment options, while the results of randomized prospective trials comparing postoperative radiotherapy versus RCHT are still awaited. [52][53][54] Various issues have so far not been resolved regarding the optimal adjuvant multimodality treatment and remain controversial, but overall, there is a need for a reasonable ratio of treatment-induced toxicity that comes along with the addition of consolidation, multiagent or stronger chemotherapy regimens, and targeted therapies. Nonetheless, reluctant approaches concerning the application of chemotherapy seem to threaten oncologic outcomes. In our study, the definition of patients who were at high risk of chemotherapy-induced toxicity was significantly age-dependent. While a deterioration of clinical performance status or hemato-and nephrotoxicity during initial postoperative RCHT led to approximately 83% of the patients receiving at least 5 and 90% at least 4 cycles in a study by Klopp et al, 44 this was in line with our results of 85.5% and 92.8%, respectively. However, there is evidence that this could be lower in up to 59.5% of patients receiving fullcourse chemotherapy, as reported by Mell et al. 55 As an alkylating agent, cisplatin affects the cell cycle and stem cells, 56 leading to acute hematologic toxicity during RCHT in cervical cancer with grade 0 + 1 / 2 + 3 anemia (86.5% / 13.5%), leukopenia (56.7% / 43.2%), and thrombocytopenia (97.3% / 2.7%) during RCHT, 55 which were also found in our cohort, showing grade 0 + 1 / 2 + 3 anemia (85.5% / 14.4%), leukopenia (62.3% / 37.7%), and thrombocytopenia (100% / 0%). We further provided new information on the absolute and relative values of blood count reductions during the course of treatment at different time points of chemotherapy cycles, indicating that the severity of cisplatin-induced anemia is maximal at the fourth cycle and that more emphasis must be placed on the prevention of limiting infections in women over 50 years due to significantly decreasing leukocyte counts from cycle 3 onwards.
The primary limitations of our analysis were caused by the retrospective nature of the study design that may impact the findings. As a consequence, our results and statistical measurements have to be interpreted cautiously, especially in the subgroup analyses, due to the small patient cohort, potential methodological issues, or confounding factors. Moreover, study limitations that arise from the retrospective design include, that the currently investigated preoperative blood cell ratios for gynecologic cancers, such as the neutrophil-to-lymphocyte ratio and systemic inflammatory response index, 25,57,58 could not be reliably assessed or confirmed due to incomplete data availability. Overall, changes or abnormal values in plasma or serum enzymes or isoenzymes and blood counts can be triggered by multicausal conditions including heart, kidney, or liver disease, and must thus be interpreted cautiously. Further systematic prospective research is needed to further validate and analyze the findings and influencing factors.
Even with the improvement and the use of technical developments, the extent of trimodality toxicity in the treatment of cervical cancer is still high, and the overall optimal adjuvant treatment scheme and chemotherapy sequence remains controversial with poor outcomes. Our data offer a new evaluation of various prognostic indices and additional insight into serologic markers and further provide a better understanding of toxicity profiles and changes during postoperative RCHT, which becomes all the more important in the ongoing discussion about the intensification and modification of systemic therapy regimens.

Conclusion
We demonstrated that full-course adjuvant concurrent RCHT for cervical cancer can improve LC; thus, age-dependent limiting factors should be identified at an early stage. For this, we advocate special emphasis on the occurrence of anemia at the time point of the fourth cycle and limiting infections as well as renal failure in women aged > 50 years. In addition to classic pathological risk factors, serological markers (CRP, LDH, nutritional index) seem a promising reliable tool for the prediction of the oncologic outcome.